Genetic/familial high-risk assessment: Colorectal version 1.2016: Clinical practice guidelines in oncology

Volume: 14, Issue: 8, Pages: 1010 - 1030
Published: Aug 1, 2016
Abstract
This is a focused update highlighting the most current NCCN Guidelines for diagnosis and management of Lynch syndrome. Lynch syndrome is the most common cause of hereditary colorectal cancer, usually resulting from a germline mutation in 1 of 4 DNA mismatch repair genes (MLH1, MSH2, MSH6, or PMS2), or deletions in the EPCAM promoter. Patients with Lynch syndrome are at an increased lifetime risk, compared with the general population, for...
Paper Details
Title
Genetic/familial high-risk assessment: Colorectal version 1.2016: Clinical practice guidelines in oncology
DOI
Published Date
Aug 1, 2016
Journal
Volume
14
Issue
8
Pages
1010 - 1030
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